Canonical Allele Identifier: CA206316
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 210299
ClinVar RCV Id: RCV000193070
dbSNP Id: rs797045280

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157206292del , CM000668.2:g.157206292del GRCh38
NC_000006.11:g.157527426del , CM000668.1:g.157527426del GRCh37
NC_000006.10:g.157569118del NCBI36
NG_032093.1:g.433363del
NG_032093.2:g.433363del
NG_066624.1:g.435267del

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.5361del ENSP00000055163.8:p.Lys1788ArgfsTer?
ENST00000414678.8:c.5430del ENSP00000412835.3:p.Lys1811ArgfsTer?
ENST00000637015.2:c.5649del ENSP00000489729.2:p.Lys1884ArgfsTer?
ENST00000346085.10:c.5400del ENSP00000344546.5:p.Lys1801ArgfsTer?
ENST00000350026.10:c.5112del ENSP00000055163.7:p.Lys1705ArgfsTer?
ENST00000414678.7:c.3678del ENSP00000412835.2:p.Lys1227ArgfsTer?
ENST00000635849.1:c.2841del ENSP00000490948.1:p.Lys948ArgfsTer?
ENST00000635957.1:c.2472del ENSP00000490385.1:p.Lys825ArgfsTer?
ENST00000636227.1:n.3983del
ENST00000636254.1:n.1440del
ENST00000636930.2:c.5520del MANE Select ENSP00000490491.2:p.Lys1841ArgfsTer?
ENST00000636940.1:n.3517del
ENST00000637015.1:c.2888del
ENST00000637568.1:c.2802del
ENST00000637741.1:n.2186del
ENST00000637810.1:c.2862del ENSP00000489636.1:p.Lys955ArgfsTer?
ENST00000637904.1:c.3021del ENSP00000490550.1:p.Lys1008ArgfsTer?
ENST00000637933.1:n.2635del
ENST00000647938.1:c.5151del ENSP00000498155.1:p.Lys1718ArgfsTer?
ENST00000346085.9:c.5151del ENSP00000344546.4:p.Lys1718ArgfsTer?
ENST00000350026.9:c.5112del ENSP00000055163.7:p.Lys1705ArgfsTer?
ENST00000414678.6:c.3678del ENSP00000412835.2:p.Lys1227ArgfsTer?
NM_017519.2:c.5112del NP_059989.2:p.Lys1705ArgfsTer?
NM_020732.3:c.5151del NP_065783.3:p.Lys1718ArgfsTer?
XM_005267069.3:c.5271del XP_005267126.2:p.Lys1758ArgfsTer?
XM_011535984.1:c.4350del XP_011534286.1:p.Lys1451ArgfsTer?
XM_011535985.1:c.4170del XP_011534287.1:p.Lys1391ArgfsTer?
XM_011535986.1:c.3930del XP_011534288.1:p.Lys1311ArgfsTer?
XM_011535987.1:c.3549del XP_011534289.1:p.Lys1184ArgfsTer?
XM_011535988.1:c.2412del XP_011534290.1:p.Lys805ArgfsTer?
NM_001346813.1:c.5271del NP_001333742.1:p.Lys1758ArgfsTer?
NM_001363725.1:c.3021del NP_001350654.1:p.Lys1008ArgfsTer?
XM_011535984.2:c.5481del XP_011534286.2:p.Lys1828ArgfsTer?
XM_011535988.3:c.2412del XP_011534290.1:p.Lys805ArgfsTer?
XM_017011103.2:c.5382del XP_016866592.1:p.Lys1795ArgfsTer?
XM_017011104.1:c.5352del XP_016866593.1:p.Lys1785ArgfsTer?
XM_017011105.2:c.5322del XP_016866594.1:p.Lys1775ArgfsTer?
XM_017011106.2:c.5193del XP_016866595.1:p.Lys1732ArgfsTer?
XM_017011107.2:c.5172del XP_016866596.1:p.Lys1725ArgfsTer?
XR_002956289.1:n.5467del
NM_001363725.2:c.3021del NP_001350654.1:p.Lys1008ArgfsTer?
NM_001371656.1:c.5400del NP_001358585.1:p.Lys1801ArgfsTer?
NM_001374820.1:c.5400del NP_001361749.1:p.Lys1801ArgfsTer?
NM_001374828.1:c.5520del MANE Select NP_001361757.1:p.Lys1841ArgfsTer?
NM_017519.3:c.5361del NP_059989.3:p.Lys1788ArgfsTer?